We’re supporting a well‑established biologics pharmaceutical organization based in Catalonia, Spain, currently undergoing a significant expansion across its manufacturing and quality operations.This position offers a strong mix of on‑site collaboration (typically 3‑4 days per week) with flexible remote working, and sit within highly regulated GMP environments across both manufacturing and corporate quality functions.This role focuses on ensuring the integrity, control, and lifecycle management of regulated pharmaceutical documentation across integral markets.Key responsibilities:Managing and maintaining GMP‑controlled documentation and recordsSupporting product registrations across multiple countriesMaintaining specifications, analytical methods, SOPs,



and change controlsEnsuring compliance with GMP and pharmacopoeia requirementsWorking closely with Quality Control and Regulatory Affairs teamsWhat we’re looking for:Strong understanding of GMP environmentsExperience with controlled quality documentation systemsFamiliarity with analytical methods and regulatory documentationStrong Microsoft Office and structured documentation skillsScientific or technical academic backgroundThis role offers the chance to join a growing international organization at a pivotal stage of expansion, with strong development opportunities across quality, validation, and corporate systems.

📌 Quality Specialist (Madrid)
🏢 Hlx Life Sciences
📍 Madrid